Allele Registry

Canonical Allele Identifier: PA2828566463

Gene: FARS2 HGNC NCBI

ClinVar RCV:

RCV000239485

ClinVar Variation:

253158

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362187.1:p.Asp281Tyr	CA10586222 NM_001375258.1:c.841G>T